6 English-speaking jobs in Rixensart

Scientific Associate will draft and review scientific documentation, collaborate with QA and RA departments, and manage quality system elements. Requires a master's degree in a scientific discipline, expertise in LC-MS and chromatography, and 2+ years of quality control experience in a GMP environment.

The Quality Control Release & Stability Testing Director is responsible for end-to-end oversight of QC release and stability testing activities for clinical products. This leader will define strategy, build and lead teams, drive technical and regulatory excellence, and partner across functions to ensure timely, compliant product release and a robust stability program.

Leads strategic initiatives to advance process and product understanding through analytical techniques. Oversees development and implementation of extended characterization platforms, including mass spectrometry, nuclear magnetic resonance, and microscopy. Builds, mentors, and leads a team of scientists. Collaborates with cross-functional teams to align characterization efforts with organizational goals. Establishes strategic collaborations with external experts and academic institutions.

The Quality Control Release & Stability Testing Director leads end-to-end oversight of QC release and stability testing activities for clinical products. This role defines strategy, builds and leads teams, drives technical and regulatory excellence, and partners across functions to ensure timely, compliant product release and a robust stability program. Responsibilities include method lifecycle management, KPI development and reporting, SOP authoring, investigation guidance, team leadership, operational management of sample receipt, testing, and data review, and ensuring compliance with GMP and regulatory requirements.

Supports formulation and drug-product development through training, document review, and project participation. Executes experiments, performs analytical testing, and analyzes data. Prepares scientific documentation and coordinates sample handling.

Develop, optimize, and qualify RP-U(H)PLC and SEC-U(H)PLC methods for antigen content determination in drug substance samples. Collaborate with internal stakeholders to support biopharmaceutical development.